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المؤلفون: Seyfeddine Zayani, Farah Thabet, Majdi Ben Massoud, Chokri Chouchane, Habib Gamra, Slaheddine Chouchane
المصدر: World Journal for Pediatric and Congenital Heart Surgery. :215013512311688
مصطلحات موضوعية: Pediatrics, Perinatology and Child Health, Surgery, General Medicine, Cardiology and Cardiovascular Medicine
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::0824b0c0fa27ea0ce23d7b913addf542Test
https://doi.org/10.1177/21501351231168868Test -
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المؤلفون: Imen Ksiaa, Habib Besbes, Moncef Khairallah, Mohamed Ghachem, Slaheddine Chouchane, Sana Khochtali
المصدر: BMC Ophthalmology, Vol 20, Iss 1, Pp 1-4 (2020)
BMC Ophthalmologyمصطلحات موضوعية: medicine.medical_specialty, Fovea Centralis, genetic structures, Retina, 03 medical and health sciences, chemistry.chemical_compound, Retinal hemorrhages, 0302 clinical medicine, Optical coherence tomography, lcsh:Ophthalmology, Ophthalmology, Vitreoretinal interface, Case report, medicine, Humans, Shaken baby syndrome, medicine.diagnostic_test, business.industry, Optic disc pallor, Retinal traction, Internal limiting membrane, Infant, Retinal Hemorrhage, Retinal, General Medicine, medicine.disease, Retinal atrophy, eye diseases, Swept source optical coherence tomography, chemistry, lcsh:RE1-994, 030221 ophthalmology & optometry, Female, sense organs, business, 030217 neurology & neurosurgery, Tomography, Optical Coherence
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::17d1297b8a93862ce3f3ba3275505a7cTest
http://link.springer.com/article/10.1186/s12886-020-01666-9Test -
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المؤلفون: Samir M'Rabet, Najoua Kahloul, Hassen Sboui, Sihem Trimech, N. Zouari, Felix G. Riepe, Mohamed Tahar Sfar, Fathi Amri, Saloua Makni, Abdelkarim Ayedi, Ali Saad, Ilhem Charfeddine, Eric Clauser, Paul-Martin Holterhus, Slaheddine Chouchane, Moez Gribaa, Hechmi Ben Hamouda
المصدر: Gene. 507(1)
مصطلحات موضوعية: Adult, Male, congenital, hereditary, and neonatal diseases and abnormalities, Tunisia, endocrine system diseases, Adolescent, Pseudogene, Population, Molecular Sequence Data, Single-nucleotide polymorphism, Steroid biosynthesis, Biology, urologic and male genital diseases, Polymorphism, Single Nucleotide, Genetics, medicine, Humans, Point Mutation, Congenital adrenal hyperplasia, Allele, education, Child, Gene, Alleles, Genetic Association Studies, education.field_of_study, Adrenal Hyperplasia, Congenital, Base Sequence, Point mutation, nutritional and metabolic diseases, Infant, General Medicine, Middle Aged, medicine.disease, Molecular biology, female genital diseases and pregnancy complications, Child, Preschool, Female, Steroid 21-Hydroxylase, Pseudogenes
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::85eea49b042f7a19bb4c8932a2e55e59Test
https://pubmed.ncbi.nlm.nih.gov/22841790Test